Canonical Allele Identifier: CA2682048226

Gene: NPY

Linked Data

• gnomAD v4: 7-24285191-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285194del , CM000669.2:g.24285194del	GRCh38
NC_000007.13:g.24324813del , CM000669.1:g.24324813del	GRCh37
NC_000007.12:g.24291338del	NCBI36
NG_016148.1:g.6007del

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-47del MANE Select	ENSP00000242152.2:n.1-47del
ENST00000242152.6:c.1-47del	ENSP00000242152.2:n.1-47del
ENST00000405982.1:c.-47del	ENSP00000385282.1:n.-47del
ENST00000407573.5:c.1-47del	ENSP00000384364.1:n.1-47del
NM_000905.3:c.1-47del	NP_000896.1:n.1-47del
XM_017012910.1:c.42-29493del	XP_016868399.1:n.42-29493del
XM_017012911.1:c.42-29493del	XP_016868400.1:n.42-29493del
XR_001745121.1:n.473+34165del
XR_001745122.1:n.345-88163del
XR_001745123.1:n.473+34165del
XR_001745124.1:n.473+34165del
XR_001745125.1:n.473+34165del
XR_001745126.1:n.473+34165del
XR_001745127.1:n.345-29493del
XR_001745129.1:n.473+34165del
XR_001745130.1:n.473+34165del
XR_001745131.1:n.473+34165del
XR_001745132.1:n.473+34165del
NM_000905.4:c.1-47del MANE Select	NP_000896.1:n.1-47del